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Randomized controlled trial of Prostate Radiotherapy In high risk and node positive disease comparing Moderate and Extreme hypofractionation PRIME Trial Randomized controlled trial of Prostate Radiotherapy
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To fill out a randomised controlled trial, follow these steps:
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Identify the research question: Determine the objective of the trial and what you aim to investigate.
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Design the trial protocol: Decide on the study design, inclusion and exclusion criteria, randomization process, intervention details, outcome measures, and sample size estimation.
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Obtain ethical approval: Seek approval from relevant ethics committees or institutional review boards.
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Recruit participants: Identify and recruit eligible participants who meet the inclusion criteria.
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Randomize participants: Randomly assign participants to either the intervention group or the control group using an appropriate randomization method.
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Implement the intervention: Administer the intervention to the participants in the intervention group as per the protocol.
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Collect data: Collect relevant data and outcome measures from both the intervention and control groups.
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Analyze the data: Use appropriate statistical methods to analyze the collected data and draw conclusions.
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Interpret the results: Interpret the findings of the trial and assess the implications for the research question.
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Report the trial: Prepare a comprehensive report of the trial, including the study design, methods, results, and conclusions.

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Randomised controlled trial is a method of study in which participants are randomly assigned to different groups to compare different treatments or interventions.
Researchers conducting clinical trials are typically required to file randomised controlled trial documents.
Randomised controlled trial documents are typically filled out with detailed information on study design, participants, interventions, outcomes, and analysis plan.
The purpose of a randomised controlled trial is to evaluate the effectiveness of different treatments or interventions in order to make evidence-based decisions in healthcare.
Information such as study protocol, study population, intervention details, outcomes, and statistical analysis plan must be reported on a randomised controlled trial.
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